Skip to main content
Log in

Reserpine Derivatives with Specific Hypotensive or Sedative Activity

  • Letter
  • Published:

From Nature

View current issue Submit your manuscript

Abstract

RECENTLY it has been reported, by Ciba Laboratories1,2, that two reserpine analogues show more specific effects than reserpine. Methyl-18-O(3-NN-dimethylaminobenzoyl)reserpate (or SU 5171) exhibits sedative activity, while carbethoxysyringoyl-methylreserpate (syrosingopine or SU 3118) is effective in decreasing blood tension (see formulæ).

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Barrett, W. E., Plummer, A. J., Rutledge, R. A., MacPhillamy, H. B., Abstracts Fall Meeting Amer. Pharm. Soc., Ann Arbor (Mich.), 3 (1958).

  2. Plummer, A. J., Barrett, W. E., Maxwell, R. A., Finocchio, D., Lucas, R. A., and Rutledge, E., Abstracts Fall Meeting Amer. Pharm. Soc., Arbor (Mien.), 27 (1958).

  3. Bogdanski, D. F., Pletscher, A., Brodie, B. B., and Udenfriend, S., J. Pharmacol. Exp. Ther., 117, 82 (1956).

    CAS  PubMed  Google Scholar 

  4. Garattini, S., and Valzelli, L., Science, 128, 1228 (1958).

    Article  ADS  Google Scholar 

  5. Shore, P. A., and Brodie, B. B., in “Psychotropic Drugs”, edit. by Garattini, S., and Ghetti, V., 423 (Elsevier Pub. Co., Amsterdam, 1957).

    Google Scholar 

  6. Darvill, jun., F. T., Ant. Med. Clin. Ther., 5, 598 (1958).

    CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

GARATTINI, S., MORTARI, A., VALSECCHI, A. et al. Reserpine Derivatives with Specific Hypotensive or Sedative Activity. Nature 183, 1273–1274 (1959). https://doi.org/10.1038/1831273a0

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1038/1831273a0

  • Springer Nature Limited

This article is cited by

Navigation